37827-68-2

Basic information

• Product Name: 7-Hydroxy-2-tetralone
• Synonyms: 7-HYDROXY-2-TETRALONE;7-HYDROXY-3,4-DIHYDRO-1H-NAPHTHALEN-2-ONE;7-Hydroxy-3,4-dihydronaphthalen-2(1H)-one;3,4-Dihydro-7-hydroxynaphthalen-2(1H)-one;7-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-one;7-hydroxy-1,2,3,4-tetrahydronaphthalen-2-one
• CAS NO: 37827-68-2
• Molecular Formula: C₁₀H₁₀O₂
• Molecular Weight: 162.19
• Mol File: 37827-68-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 353.3°C at 760 mmHg
• Flash Point: 150.6°C
• Appearance: /
• Density: 1.236g/cm³
• Vapor Pressure: 1.77E-05mmHg at 25°C
• Refractive Index: 1.602
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 7-Hydroxy-2-tetralone(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Hydroxy-2-tetralone(37827-68-2)
• EPA Substance Registry System: 7-Hydroxy-2-tetralone(37827-68-2)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 22
• Safety Statements: 26-36
• Hazardous Substances Data: 37827-68-2(Hazardous Substances Data)

Usage

General Description

7-Hydroxy-2-tetralone is a chemical compound with the molecular formula C10H10O2. It is a derivative of tetralone that contains a hydroxyl group at the 7th position. It is a yellow crystalline solid that is used in the synthesis of pharmaceuticals and organic compounds. Its applications include its use as a building block for the synthesis of various natural products and pharmaceuticals. The compound has been studied for its potential biological activities, including its antioxidant and anti-inflammatory properties. Overall, 7-Hydroxy-2-tetralone is a versatile chemical with potential applications in the pharmaceutical and research industries.

InChI:InChI=1/C10H10O2/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/h1,3,5,11H,2,4,6H2

Upstream product

• 208932-51-8 3-(4-hydroxyphenyl)propionic acid allyl ester 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 4133-34-0 7-methoxyl-2-tetralone 
• 108-98-5 thiophenol 
• 582-17-2 2,7-Dihydroxynaphthalene 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 501-97-3 4-hydroxyphenylpropionic acid 
• 66628-99-7 3-(4-hydroxyphenyl)propanoyl chloride 

Downstream Products

• 84344-52-5 7-[3-(4-Phenyl-piperazin-1-yl)-propoxy]-3,4-dihydro-1H-naphthalen-2-one 
• 1374428-94-0 (S)-1,2,3,4-tetrahydronaphthalene-2,7-diyl bis(4-bromobenzoate) 
• 41363-00-2 7-OH-AT 

Relevant articles and documents

6-SUBSTITUTED NICOTINAMIDE DERIVATIVES AS OPIOID RECEPTOR ANTAGONISTS

A compound of the formula (I) or a pharmaceutically acceptable salt, enantiomer, racemate, diastereomers or mixtures thereof, or a solvate thereof, formulations and methods of use thereof, as opioid receptor antagonists are disclosed wherein the variables are as described herein.

Ionic hydrogenation of dihydroxynaphthalenes with cyclohexane in the presence of aluminum bromide

Reactions of 1,5-, 1,6-, 1,7-, 2,6-, and 2,7-dihydroxynaphthalenes with cyclohexane in the presence of excess aluminum bromide in methylene bromide quantitatively yield 5-, 6-, and 7-hydroxynaphthalen-1-ones and 6- and 7-hydroxynaphthalen-2-ones, respectively. Tricationic C-protonated complexes are presumed to be reactive intermediates in these processes.